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FDA 510(k)

SUCTION SAFETY DEVICE

K-Number: K960937 · 1996-06-05

ApplicantR D Intl.
Decision Date1996-06-05
Product CodeMJJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUCTION SAFETY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is R D Intl.. It received FDA 510(k) clearance on 1996-06-05 under 510(k) number K960937. The device is classified under product code MJJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION SAFETY DEVICE?

SUCTION SAFETY DEVICE is a medical device that received FDA 510(k) clearance on 1996-06-05. The listed applicant is R D Intl.. The 510(k) number is K960937.

When did SUCTION SAFETY DEVICE receive FDA 510(k) clearance?

SUCTION SAFETY DEVICE received FDA 510(k) clearance on 1996-06-05, under 510(k) number K960937.

Who is the listed applicant for SUCTION SAFETY DEVICE?

The FDA 510(k) record lists R D Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION SAFETY DEVICE?

The FDA product code for SUCTION SAFETY DEVICE is MJJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing R D Intl. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960312RDI CARDIAC INSULATION PAD

Related Devices (Code: MJJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K182442MiniGuard Arterial Safety ValveQuest Medical, Inc.K0012453T L. V. CONTROL VALVE3t Medical Systems, LLCK992785IBC FLOGUARD, MODEL 6050International Biophysics Corp.K982406COBE VACUUM RELIEF CHECK VALVECobe Cardiovascular, Inc.K922781FLOW CONROL VALVEAmerican Omni Medical, Inc.K922356FLOW CONTROL VALVE, CAT. NO. ACV-38American Omni Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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